anti c3b ic3b sections (Vector Laboratories)


92
Name:
VECTASHIELD Hardset Antifade Mounting Medium with DAPI
Description:
VECTASHIELD Antifade Mounting Medium is a unique stable formula for preserving fluorescence VECTASHIELD Mounting Medium prevents rapid photobleaching of fluorescent proteins and fluorescent dyes Features Inhibits photobleaching of dyes and fluorescent proteins Ideal refractive index Ready to use No warming necessary Offered with nuclear or cytoskeletal counterstains Available in non hardening or hardening formulations Can be stored without sealing for long term analysis Easy to useVECTASHIELD HardSet Mounting Medium preserves fluorescence and hardens after coverslipping After approximately 15 minutes at room temperature the coverslip will become immobilized and optimal antifade ability and refractive index will be achieved
Catalog Number:
h-1500
Price:
None
Size:
10 ml
Category:
Histology reagents or solutions or stains
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Structured Review
Vector Laboratories
anti c3b ic3b sections

VECTASHIELD Antifade Mounting Medium is a unique stable formula for preserving fluorescence VECTASHIELD Mounting Medium prevents rapid photobleaching of fluorescent proteins and fluorescent dyes Features Inhibits photobleaching of dyes and fluorescent proteins Ideal refractive index Ready to use No warming necessary Offered with nuclear or cytoskeletal counterstains Available in non hardening or hardening formulations Can be stored without sealing for long term analysis Easy to useVECTASHIELD HardSet Mounting Medium preserves fluorescence and hardens after coverslipping After approximately 15 minutes at room temperature the coverslip will become immobilized and optimal antifade ability and refractive index will be achieved
https://www.bioz.com/result/anti c3b ic3b sections/product/Vector Laboratories
Average 92 stars, based on 1115 article reviews
Price from $9.99 to $1999.99

VECTASHIELD Antifade Mounting Medium is a unique stable formula for preserving fluorescence VECTASHIELD Mounting Medium prevents rapid photobleaching of fluorescent proteins and fluorescent dyes Features Inhibits photobleaching of dyes and fluorescent proteins Ideal refractive index Ready to use No warming necessary Offered with nuclear or cytoskeletal counterstains Available in non hardening or hardening formulations Can be stored without sealing for long term analysis Easy to useVECTASHIELD HardSet Mounting Medium preserves fluorescence and hardens after coverslipping After approximately 15 minutes at room temperature the coverslip will become immobilized and optimal antifade ability and refractive index will be achieved
https://www.bioz.com/result/anti c3b ic3b sections/product/Vector Laboratories
Average 92 stars, based on 1115 article reviews
Price from $9.99 to $1999.99
anti c3b ic3b sections - by Bioz Stars,
2021-02
92/100 stars
Related Products / Commonly Used Together
Images
1) Product Images from "Monoclonal Antibodies Capable of Inhibiting Complement Downstream of C5 in Multiple Species"
Article Title: Monoclonal Antibodies Capable of Inhibiting Complement Downstream of C5 in Multiple Species
Journal: Frontiers in Immunology
doi: 10.3389/fimmu.2020.612402

Figure Legend Snippet: Testing anti-C7 mAbs in vivo . (A) mAb 73D1 or BB5.1 anti-mouse C5 as positive control was administered IP at a dose of 1 mg/kg to female wildtype mice (n=5 per group); blood was sampled at intervals serum obtained and added to human C7D or C5D serum respectively prior to measuring CP hemolytic activity measured. Controls included C7D and C5D human sera at the same dose, NMS to demonstrate the requirement for human depleted sera and 1% Tween-20 and HBS to set 100% and 0% lysis in the assay. Significance of differences between groups was determined by one-way ANOVA; significant differences and p values are shown in the figure. Error bars are standard errors of triplicates. (B) C7-deficient mice (10 females) were reconstituted with human C7 (500µg; IP), then split into test and control groups (5 in each). After 1 h, test and control animals were injected subcutaneously (SC) with 17E7 mAb or irrelevant isotype control mAb (1 mg) respectively. Blood was collected prior to administration of C7, immediately prior to administration of mAb and 3 h after mAb administration. Hemolytic activity was measured as above. Significance of differences between groups was determined using an unpaired t test; significant differences and p values are shown in the figure. Error bars are standard errors of triplicates. (C) Female Lewis rats were divided into three groups (n = 2 each) and injected intraperitoneally with mAb 2H2 at doses of 10, 20, and 40 mg/kg; blood was collected from all the animals just before mAb administration, 2 h after mAb 2H2 administration, and then every 12 h over 1 week. Sera prepared and hemolytic activity tested in standard CP assays. Significance of differences between groups was determined using an unpaired t test; significant differences and p values are shown in the figure. Error bars are standard errors of triplicates. (D–F) EAMG was induced in rats (5 per group) and either mAb 2H2 or isotype control mAb(10mg/kg) administered at induction. Weight loss (D) and clinical score (E) were measured at intervals; mice were bled at 0, 2, 24, and 48 h, serum harvested and hemolytic activity measured (F) . All animals were killed at 48 h. Results are means of five in each group and vertical bars represent SD. Significance of differences between groups was determined using an unpaired t test except panel E where paired t test was used; significant differences and p values are shown in the figures. (G–K). Soleus muscles were harvested at time of sacrifice (48 h) and snap frozen in OCT. Sections (10 µm) were stained for AChR with TRITC-conjugated a-BuTX; AChR-positive endplates were counted in 10 fields from each animal using ImageJ software. (G) . Sections were stained for C3b/iC3b (H) and C9/MAC (I) and staining quantified as above. Tissue sections from isotype control (J) or 2H2 (K) treated animals were double-stained for AChR together with anti-C3b/iC3b (top panel) or C9/MAC (bottom panel) and imaged on a Zeiss confocal microscope. The scale bar shown is 10 µm; all images were captured at identical magnification. Statistical significance was obtained by unpaired t-test and P
Techniques Used: In Vivo, Positive Control, Mouse Assay, Activity Assay, Lysis, Injection, Staining, Software, Microscopy
2) Product Images from "Cancer Stem Cells in Head and Neck Cutaneous Squamous Cell Carcinoma Express Cathepsins"
Article Title: Cancer Stem Cells in Head and Neck Cutaneous Squamous Cell Carcinoma Express Cathepsins
Journal: Plastic and Reconstructive Surgery Global Open
doi: 10.1097/GOX.0000000000003042

Figure Legend Snippet: Representative immunofluorescence sections of moderately differentiated head and neck squamous cell carcinoma tissue samples demonstrating expression of cathepsin B (A, D, red) by the c-MYC + (A, green) cells within the tumor nests (TNs) (A, arrows), as well as cells in the peritumoral stroma (PTS) (A, arrowheads). The cells within the PTS are both OCT4 + (D, green, arrows) and OCT4 − (D, red, arrowheads). Similarly, cathepsin D (B, E, red) was also expressed by the c-MYC + (B, green) cells within the TNs (B, arrows) and the PTS (B, arrowheads), as well as both the OCT4 + (E, green, arrows) and OCT4 − (E, red, arrowheads) cells of the PTS. Cathepsin G (C, F, red) was expressed by some c-MYC + (C, green, arrows) cells within the PTS, but not by the OCT4 + (F, green) cells. Tryptase + (G, green) cells within the PTS also expressed cathepsin G (G, red). All slides were counter-stained with 4′,6′-diamino-2-phenylindole. Original magnification: ×400. Scale bar: 20 µm.
Techniques Used: Immunofluorescence, Expressing, Staining
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